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1,1-dibutyl-3-(3-methyl-1,1-dioxidotetrahydrothiophen-3-yl)urea is a complex organic compound with the molecular formula C15H26N2O3S2. It is a derivative of urea, featuring a 1,1-dibutyl group and a 3-methyl-1,1-dioxidotetrahydrothiophen-3-yl moiety. 1,1-dibutyl-3-(3-methyl-1,1-dioxidotetrahydrothiophen-3-yl)urea is characterized by its unique structure, which includes a sulfur-containing heterocyclic ring and a urea functional group. It is synthesized through a series of chemical reactions and is used in various applications, such as in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its specific chemical properties, it is essential to handle 1,1-dibutyl-3-(3-methyl-1,1-dioxidotetrahydrothiophen-3-yl)urea with care, following proper safety protocols and guidelines.

5155-77-1

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5155-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5155-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5155-77:
(6*5)+(5*1)+(4*5)+(3*5)+(2*7)+(1*7)=91
91 % 10 = 1
So 5155-77-1 is a valid CAS Registry Number.

5155-77-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dibutyl-3-(3-methyl-1,1-dioxothiolan-3-yl)urea

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:5155-77-1 SDS

5155-77-1Downstream Products

5155-77-1Relevant academic research and scientific papers

The Oxidative-Rearrangement of 1-Amino-2-indolinones. A Synthesis of 2-Substituted-3(2H)-cinnolinones.

Zey, R.L.,Richter, G.,Randa, H.

, p. 1437 - 1439 (2007/10/02)

Several 2-substituted-3(2H)-cinnolinones have been synthesized by a ring expansion of the respective 1-substituted-2-indolinones via an oxidative-rearrangement with t-butyl hypochlorite.

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